ISO 13485:2016 Standard for Quality management systems — Requirements for regulatory purposes »
ISO 13485:2016 Standard- Table of contents
The book is organized like the standard itself, the table of contents is identical to the ISO 13485 Standards table of contents making it user friendly, familiar, and unintimidating. Each chapter contains the information,
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Why choose the book ISO 13485:2016 – A Complete Guide to Quality Management in the Medical Device Industry
Why choose the book ISO 13485:2016 – A Complete Guide to Quality Management in the Medical Device Industry over other menu scripts? When you’ve done as much as I have in the quality management
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Introducing the project ISO 13485:2016 – A Complete Guide to Quality Management in the Medical Device Industry
The quality management world of the medical device industry has gone through a significant change represented by the publication of the new revision of the ISO 13485 Standard, the 2016 revision. This revision brings
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